Dai Qiong, Yan Yan, Guo Junling, Björnmalm Mattias, Cui Jiwei, Sun Huanli, Caruso Frank
ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, and the Department of Chemical and Biomolecular Engineering, The University of Melbourne, Parkville, Victoria 3010, Australia.
ACS Macro Lett. 2015 Nov 17;4(11):1259-1263. doi: 10.1021/acsmacrolett.5b00627. Epub 2015 Oct 30.
Protein coronas formed on engineered particles can alter their targeting ability as they enter biological environments. Here, we engineer polymer-coated silica particles and investigate the influence of protein coronas derived from various sources. The particles were functionalized with a small antibody-mimetic ligand (affibody), and their targeting ability to cancer cells in the presence of protein coronas was determined. Protein coronas derived from human serum showed a dramatic inhibition of specific particle-cell association (from ∼70 to ∼7%), whereas the most abundant protein in human serum-human serum albumin-enhanced the specific association of functionalized particles to SK-OV-3 human ovary cancer cells (to ∼90%). This study shows how protein coronas can both facilitate and impede targeting and provides key insights into the importance of challenging engineered particles with multicomponent biologically relevant environments.
工程颗粒表面形成的蛋白质冠层在进入生物环境时会改变其靶向能力。在此,我们设计了聚合物包覆的二氧化硅颗粒,并研究了源自各种来源的蛋白质冠层的影响。这些颗粒用一种小型抗体模拟配体(亲和体)进行功能化处理,并测定了它们在存在蛋白质冠层的情况下对癌细胞的靶向能力。源自人血清的蛋白质冠层显著抑制了颗粒与细胞的特异性结合(从约70%降至约7%),而人血清中最丰富的蛋白质——人血清白蛋白——增强了功能化颗粒与SK-OV-3人卵巢癌细胞的特异性结合(至约90%)。这项研究展示了蛋白质冠层如何既能促进也能阻碍靶向作用,并为在多组分生物相关环境中对工程颗粒进行挑战的重要性提供了关键见解。